3.8 Article

MObility ImproVEment with spasticity in multiple sclerosis in Europe: the MOVE 1 EU study

期刊

NEURODEGENERATIVE DISEASE MANAGEMENT
卷 4, 期 6, 页码 407-415

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/NMT.14.44

关键词

activities of daily living; burden of disease; EU; multiple sclerosis; pharmacotherapy; quality of life; spasticity; symptoms; treatment satisfaction

资金

  1. Biogen-Idec
  2. Merck-Serono
  3. Novartis
  4. Bayer-Schering
  5. Sanofi-Genzyme
  6. Teva
  7. Almirall
  8. Almirall SA (Barcelona, Spain)

向作者/读者索取更多资源

Aim: using a protocol similar to that of the MOVE 1 study in Germany, the multicenter, observational MOVE 1 EU study examined the burden of multiple sclerosis (MS)-related spasticity in other EU countries (Belgium, Finland, France, Ireland, Norway, Poland and Portugal). Materials & Methods: A 12-month retrospective chart documentation was combined with questionnaires for physicians and patients at the time of enrollment. A total of 281 patients from neurology departments and MS units formed the per protocol population. Results: in most patients, MS spasticity frequently restricted daily activities and caused some/moderate problems in EQ-5D subdomains of mobility, usual activities and pain/discomfort. Overall, 48% of physicians and 34% of patients were at least partly dissatisfied with the effectiveness of available pharmacotherapy options for MS spasticity. Conclusion: Results of the MOVE 1 Germany and MOVE 1 EU studies are aligned and highlight the need to optimize the therapeutic management of patients with MS spasticity across Europe so as to improve their overall well-being and quality of life.

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